Lack of thyroid hormone receptor alpha1 is associated with selective alterations in behavior and hippocampal circuits

• Published in: Molecular psychiatry Vol. 8; no. 1; pp. 30 - 38
• Main Authors: Guadaño-Ferraz, A, Benavides-Piccione, R, Venero, C, Lancha, C, Vennström, B, Sandi, C, DeFelipe, J, Bernal, J
• Format: Journal Article
• Language: English
• Published: England 01.01.2003
• Subjects: Animals; Behavior, Animal - physiology; Conditioning (Psychology) - physiology; Fear - physiology; gamma-Aminobutyric Acid - physiology; Hippocampus - chemistry; Hippocampus - cytology; Hippocampus - physiology; Interneurons - chemistry; Interneurons - physiology; Male; Medicin och hälsovetenskap; Memory - physiology; Mice; Mice, Inbred BALB C; Mice, Mutant Strains; Neural Inhibition - physiology; Parvalbumins - analysis; Pyramidal Cells - chemistry; Pyramidal Cells - physiology; Thyroid Hormone Receptors alpha - analysis; Thyroid Hormone Receptors alpha - genetics; Thyroid Hormones - analysis
• ISSN: 1359-4184
• DOI: 10.1038/sj.mp.4001196

Brain development and function are dependent on thyroid hormone (T3), which acts through nuclear hormone receptors. T3 receptors (TRs) are transcription factors that activate or suppress target gene expression in a hormone-dependent or -independent fashion. Two distinct genes, TRalpha and TRbeta, encode several receptor isoforms with specific functions defined in many tissues but not in the brain. Mutations in the TRbeta gene cause the syndrome of peripheral resistance to thyroid hormone; however, no alterations of the TRalpha gene have been described in humans. Here we demonstrate that mice lacking the TRalpha1 isoform display behavioral abnormalities of hippocampal origin, as shown by the open field and fear conditioning tests. In the open field test mutant mice revealed less exploratory behavior than wild-type mice. In the contextual fear conditioning test mutant mice showed a significantly higher freezing response than wild-type controls when tested 1 week after training. These findings correlated with fewer GABAergic terminals on the CA1 pyramidal neurons in the mutant mice. Our results indicate that TRalpha1 is involved in the regulation of hippocampal structure and function, and raise the possibility that deletions or mutations of this receptor isoform may lead to behavioral changes or even psychiatric syndromes in humans.